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基于磁辅助生物素化单链可变片段抗体的金刚烷胺免疫分析方法用于鸡肉中金刚烷胺的检测。

Magnetic-assisted biotinylated single-chain variable fragment antibody-based immunoassay for amantadine detection in chicken.

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, People's Republic of China.

Beijing Key Laboratory of Detection Technology for Animal-Derived Food Safety, Beijing Laboratory for Food Quality and Safety, Beijing, 100193, People's Republic of China.

出版信息

Anal Bioanal Chem. 2018 Sep;410(24):6197-6205. doi: 10.1007/s00216-018-1227-z. Epub 2018 Jul 14.

Abstract

A sensitive competitive immunoassay with simple operation was developed for the detection of the anti-virus drug amantadine (AMD). The single-chain variable fragment (scFv) antibody against AMD was site-specific biotinylated and overexpressed as a secreted body in Escherichia coli AVB101. Horseradish peroxidase-labeled streptavidin-biotinylated scFv antibody (HRP-SA-BIO-scFv) could specifically bind to AMD-functionalized magnetic beads (MBs) and then the immune complexes were separated from the matrix solution by magnet. The concentration of the AMD could be known by the measurement of the signal produced by the horseradish peroxidase. The newly established assay provides a significant improvement in comparison to the conventional ELISA without SA-BIO signal amplification and MBs separation. The limit of detection and assay time was 0.64 vs. 8.4 ng/mL and 50 vs. 150 min, respectively. The recoveries ranged from 77.8 to 112% with the coefficient of variation less than 13%. The immunoassay exhibited an obvious cross-reactivity to rimantadine (84%), 1-(1-adamantyl)ethylamine (72%), and somantadine (63%). These results demonstrated that the developed immunoassay provided a sensitive, rapid, and accurate approach for the detection of AMD in chicken by employing MBs as solid phase and SA-BIO as signal amplification. When applied in natural chicken samples, the newly established method provided results consistent with those from UPLC-MS/MS, suggesting that the proposed method could be used for rapid screening of the target of interest; the new immunoassay could also be extended to other small molecular contaminants and thus represents a universal strategy for food safety analysis. Graphical abstract ᅟ.

摘要

建立了一种用于检测抗病毒药物金刚烷胺 (AMD) 的简单操作、高灵敏度的竞争免疫分析法。AMD 单链可变片段 (scFv) 抗体经定点生物素化后,在大肠杆菌 AVB101 中作为分泌体过表达。辣根过氧化物酶标记的链霉亲和素-生物素化 scFv 抗体 (HRP-SA-BIO-scFv) 可特异性结合到 AMD 功能化磁珠 (MBs) 上,然后通过磁场将免疫复合物从基质溶液中分离出来。通过测量辣根过氧化物酶产生的信号,可以得知 AMD 的浓度。与没有 SA-BIO 信号放大和 MBs 分离的传统 ELISA 相比,新建立的测定方法有了显著的改进。检测限和检测时间分别为 0.64 和 50 ng/mL 比 8.4 ng/mL 和 150 min。回收率在 77.8%到 112%之间,变异系数小于 13%。该免疫分析对金刚烷胺 (84%)、1-(1-金刚烷基)乙胺 (72%) 和索马坦丁 (63%) 表现出明显的交叉反应性。这些结果表明,该免疫分析方法通过将 MBs 作为固相和 SA-BIO 作为信号放大,为检测鸡肉中的 AMD 提供了一种灵敏、快速、准确的方法。当应用于天然鸡肉样品时,新建立的方法与 UPLC-MS/MS 的结果一致,表明该方法可用于快速筛选目标物;新的免疫分析法也可以扩展到其他小分子污染物,因此代表了食品安全分析的通用策略。

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